Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family
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Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@ast
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@en
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@en-gb
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@nl
type
label
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@ast
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@en
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@en-gb
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@nl
prefLabel
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@ast
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@en
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@en-gb
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@nl
P2093
P2860
P3181
P356
P1476
Exome sequencing identifies a ...... oss DFNA4B in a Chinese family
@en
P2093
Chufeng He
Hailin Zhang
Honghan Wang
Hongsheng Chen
Jianguo Zhang
Jianjun Yu
Jingjing Xiao
P2860
P2888
P304
P3181
P356
10.1038/JHG.2014.114
P407
P50
P577
2015-01-15T00:00:00Z
P5875
P6179
1052894681